A deazariboflavin chromophore kinetically stabilizes reduced FAD state in a bifunctional cryptochrome

Sci Rep. 2023 Oct 4;13(1):16682. doi: 10.1038/s41598-023-43930-0.

Abstract

An animal-like cryptochrome derived from Chlamydomonas reinhardtii (CraCRY) is a bifunctional flavoenzyme harboring flavin adenine dinucleotide (FAD) as a photoreceptive/catalytic center and functions both in the regulation of gene transcription and the repair of UV-induced DNA lesions in a light-dependent manner, using different FAD redox states. To address how CraCRY stabilizes the physiologically relevant redox state of FAD, we investigated the thermodynamic and kinetic stability of the two-electron reduced anionic FAD state (FADH-) in CraCRY and related (6-4) photolyases. The thermodynamic stability of FADH- remained almost the same compared to that of all tested proteins. However, the kinetic stability of FADH- varied remarkably depending on the local structure of the secondary pocket, where an auxiliary chromophore, 8-hydroxy-7,8-didemethyl-5-deazariboflavin (8-HDF), can be accommodated. The observed effect of 8-HDF uptake on the enhancement of the kinetic stability of FADH- suggests an essential role of 8-HDF in the bifunctionality of CraCRY.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chlamydomonas reinhardtii* / metabolism
  • Cryptochromes / metabolism
  • Deoxyribodipyrimidine Photo-Lyase* / metabolism
  • Flavin-Adenine Dinucleotide / metabolism
  • Oxidation-Reduction

Substances

  • Cryptochromes
  • Flavin-Adenine Dinucleotide
  • Deoxyribodipyrimidine Photo-Lyase